Fotemustine |
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| Trade names | Mustophoran |
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| AHFS/Drugs.com | International Drug Names |
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| Legal status |
- AU: S4 (Prescription only)
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(RS)-diethyl (1-{[(2-chloroethyl)(nitroso)carbamoyl]amino} ethyl)phosphonate
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| CompTox Dashboard (EPA) | |
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| ECHA InfoCard | 100.158.792 |
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| Formula | C9H19ClN3O5P |
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| Molar mass | 315.69 g·mol−1 |
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| 3D model (JSmol) | |
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O=P(OCC)(OCC)C(NC(=O)N(N=O)CCCl)C
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InChI=1S/C9H19ClN3O5P/c1-4-17-19(16,18-5-2)8(3)11-9(14)13(12-15)7-6-10/h8H,4-7H2,1-3H3,(H,11,14) YKey:YAKWPXVTIGTRJH-UHFFFAOYSA-N Y
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N Y (what is this?) (verify) |
Fotemustine is a nitrosourea alkylating agent used in the treatment of metastatic melanoma. It is available in Europe but has not been approved by the United States FDA.[1] A study[2] has shown that fotemustine produces improved response rates but does not increase survival (over dacarbazine in the treatment of disseminated cutaneous melanoma. Median survival was 7.3 months with fotemustine versus 5.6 months with DTIC (P=.067). There was also toxicity prevalence in fotemustine arm. The main toxicity was grade 3 to 4 neutropenia (51% with fotemustine v 5% with DTIC) and thrombocytopenia (43% v 6%, respectively).
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Intracellular chemotherapeutic agents / antineoplastic agents (L01) |
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SPs/MIs (M phase) | | Block microtubule assembly | |
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| Block microtubule disassembly |
- Taxanes (Cabazitaxel
- Docetaxel#
- Larotaxel
- Ortataxel†
- Paclitaxel#
- Tesetaxel)
- Epothilones (Ixabepilone)
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DNA replication inhibitor | DNA precursors/ antimetabolites (S phase) | | Folic acid | |
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| Purine | |
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| Pyrimidine |
- DNA polymerase inhibitor (Cytarabine# +daunorubicin)
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| Deoxyribonucleotide | |
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Topoisomerase inhibitors (S phase) | | I |
- Camptotheca (Belotecan
- Camptothecin
- Cositecan†
- Etirinotecan pegol†
- Exatecan
- Gimatecan
- Irinotecan#
- Lurtotecan‡
- Rubitecan‡
- Silatecan§
- Topotecan)
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| II | |
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| II+Intercalation | |
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Crosslinking of DNA (CCNS) | | Alkylating | |
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| Platinum-based | |
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| Nonclassical | |
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| Intercalation | |
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| Photosensitizers/PDT | |
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| Other | | Enzyme inhibitors |
- FI (Tipifarnib§)
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- PIKI (Pi3K) (Alpelisib
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- Duvelisib
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- Inavolisib
- Umbralisib‡)
- IDH (Enasidenib
- Ivosidenib
- Olutasidenib
- Vorasidenib)
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| Receptor antagonists | |
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| Other/ungrouped |
- Adagrasib
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- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III
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